“…The title compound (1) was prepared by oxidation of 4-phenyl-6,7,8,9-tetrahydro-lH-2,3-benzodiazepine (2) using m-chloroperbenzoic acid (m-CPBA) (Argo, Robertson & Sharp, 1984). The barrier to ring inversion in the diazepine ring of the oxide (1) is substantially reduced by about 15 kJ mo1-1 compared with the parent diazepine (2) as determined by variable-temperature 1H NMR studies.…”